Disclosed is a glass fiber-reinforced composition, which comprises (A) 99-40 wt. % of a modified ethylene/propylene block copolymer having a polar monomer content of at least 0.05 wt. %, which is obtained by graft-modifying at least partially a crystalline ethylene/propylene block copolymer, in which the ethylene content is 3-15 wt. %, the melt flow rate is 0.1 to 70 g/10 min, the intrinsic viscosity of the portion soluble in p-xylene at normal temperature is 2.5-6 as measured in decalin at 135°C and the ethylene content of the portion insoluble in p-xylene at normal temperature is 1.5-10 wt. %, with a polar monomer and an organic peroxide in an extruder, (B) up to 20 wt. % of a polyolefin rubber, and (C) 1 to 45 wt. % of a surface-treated glass fiber. This composition gives a molded article having an excellent rigidity and impact resistance.
|
1. A glass fiber-reinforced polypropylene composition, which comprises, based on the total weight of the composition:
(A) 99 to 40% by weight of a modified ethylene/propylene block copolymer having an itaconic anhydride content of at least 0.5% by weight, which is obtained by graft-modified at least a part of a crystalline ethylene/propylene block copolymer, in which the ethylene content is 3 to 15% by weight, the melt flow rate is 0.1 to 70 g/10 min., the intrinsic viscosity of the portion soluble in p-xylene at normal temperature is 2.5 to 6 as measured in dacalin at 135°C. and the ethylene content of the portion insoluble in p-xylene at normal temperature is 1.5 to 10% by weight, with itaconic anhydride and an organic peroxide in an extruder, (B) 0 to 20% by weight of a polyolefin rubber, and (C) 1 to 45% by weight of a surface-treated glass fiber.
2. A composition as set forth in
3. A composition as set forth in
4. A composition as set forth in
5. A composition as set forth in
6. A composition as set forth in
7. A composition as set forth in
8. A composition as set forth in
|
|||||||||||||||||||||||||||
cl BACKGROUND OF THE INVENTION
(1) Field of the Invention
The present invention relates to a glass fiber-reinforced polypropylene composition which gives a molded article having excellent rigidity and impact resistance.
(2) Description of the Related Art
Polypropylene has ekcellent physical and chemical properties and is widely used for electric appliances, construction materials, automobile parts, and parts of various machines.
In fields where high rigidity is required, various fillers are incorporated into polypropylene, and in fields where an especially high rigidity is necessary, glass fiber-reinforced polypropylene is used.
Glass fiber-reinforced polypropylene is unsatisfactory in touch and appearance because the glass fiber rises on the surface of a molded article, the gloss of the surface is poor, and the surface is rough and gritty. Further, the impact resistance is low, and accordingly, the commercial value is low.
To improve the physical properties of glass fiber-reinforced polypropylene, a resin composition has been proposed wherein polypropylene grafted with maleic anhydride is substituted for the polypropylene (see Japanese Examined Patent Publication No. 51-10265). This resin composition, however, has a low impact resistance and accordingly, the commercial value is low.
Accordingly, to improve the impact resistance of a molded article of glass fiber-reinforced polypropylene, a composition has been proposed in which a linear amorphous rubbery polymer is incorporated into polypropylene (see Japanese Examined Patent Publication No. 59-2294). This composition comprises 40 to 85 parts by weight of crystalline polypropylene grafted with a polar vinyl monomer or other crystalline polyolefin, 5 to 50 parts by weight of a glass fiber, and 5 to 35 parts by weight of a linear amorphous rubbery elastomer. However, this composition is not preferred from the practical viewpoint because the composition has a poor impact resistance, especially a drop weight impact strength which is an important factor in practice.
It is a primary object of the present invention to solve the above-mentioned problems involved in the conventional glass fiber-reinforced polypropylene compositions and provide a composition that can give a glass fiber-reinforced polypropylene molded article having high rigidity and high impact resistance, especially a high drop weight impact resistance.
More specifically, in accordance with the present invention, there is provided a glass fiber-reinforced polypropylene composition, which comprises, based on the total weight of the composition, (A) 99 to 40% by weight of a modified ethylene/propylene block copolymer having a polar monomer content of at least 0.05% by weight, which is obtained by graft-modifying at least a part of a crystalline ethylene/propylene block copolymer, in which the ethylene content is 3 to 15% by weight, the melt flow rate is 0.1 to 70 g/10 min, the intrinsic viscosity of the portion soluble in p-xylene at normal temperature is 2.5 to 6 as measured in decalin at 135°C (the same will apply hereinafter) and the ethylene content of the portion insoluble in p-xyIene at normal temperature is 1.5 to 10% by weight, with a polar monomer and an organic peroxide in an extruder, (B) up to 20% by weight of a polyolefin rubber, and (C) 1 to 45% by weight of a surface-treated glass fiber.
According to the present invention, since graft modification can be carried out in an extruder even though a crystalline ethylene/propylene block copolymer is used in substitution for polypropylene, a polypropylene composition having an excellent rigidity and impact resistance can be obtained by a simple operation.
In the present invention, a modified ethylene/propylene block copolymer which is at least partially graft-modified with a polar monomer and has a polar monomer content of at least 0.05% by weight is used in substitution for the polypropylene. The polyolefin used in the present invention for obtaining the modified ethylene/propylene block copolymer is a crystalline ethylene/propylene block copolymer in which the ethylene content is 3 to 15% by weight, the melt flow rate (MFR) is 0.1 to 70 g/10 min, preferably 0.3 to 20 g/10 min (ASTM D-1238, 230°C, 2160 g), the intrinsic viscosity of the portion soluble in p-xylene at normal temperature (preferably in an amount of 5 to 25% by weight) is 2.5 to 6, preferably 3 to 5, and the ethylene content of the portion insoluble in p-xylene at normal temperature (preferably in an amount of 75 to 95% by weight) is 1.5 to 10% by weight, preferably 3 to 7% by weight. If the total ethylene content or the ethylene content of the portion insoluble in p-xylene at normal temperature is too low and below the above-mentioned range, the impact resistance of the obtained composition is low. In contrast, if the ethylene content exceeds the upper limit, the ethylene component is crosslinked during the graft modification carried out in an extruder, and the impact resistance is reduced and the appearance of the molded article degraded. If the intrinsic viscosity of the portion soluble in p-xylene at normal temperature is lower than the lower limit, the impact resistance of the composition is low. In contrast, if this intrinsic viscosity is higher than the upper limit, crosslinking is readily caused in an extruder and the impact resistance of the obtained composition is reduced. It is difficult to prepare polypropylene having an MFR lower than the above-mentioned lower limit, and if the MFR exceeds the upper limit, pelletization after the graft modification in an extruder is difficult and handling is not easy.
The crystalline ethylene/propylene block copolymer is graft-modified by melt-mixing the copolymer with a polar monomer and an organic peroxide in an extruder, preferably at 175° to 280°C for about 1 to about 20 minutes.
The polar monomer is not particularly critical. Unsaturated carboxylic acids and their functional derivatives, such as itaconic anhydride, maleic anhydride, acrylic acid and derivatives thereof can be mentioned. Of these, itaconic anhydride is preferred.
The organic peroxide is not particularly critical. An organic peroxide in which the decomposition temperature giving a half value period of 1 minute is not lower than the melting point of the crystalline ethylene/propylene block copolymer used and not higher than 220°C is preferred. For example, there can be mentioned t-butyl peroxybenzoate, cyclohexanone peroxide, 2,5-dimethyl-2,5-di(benzoylperoxy)hexane, t-butyl peroxyacetate, methyl ethyl ketone peroxide, dicumyl peroxide and 2,5-dimethyl-2,5-di(t-butylperoxy)hexane.
Preferably, the graft polymerization can be accomplished by mixing 100 parts by weight of the crystalline ethylene/propylene block copolymer with 0.05 to 3 parts by weight of the polar monomer and 0.002 to 1 part by weight of the organic peroxide and melt-kneading the mixture in nitrogen or air. It is preferred that pelletization be carried out after the graft modification in the extruder. The resultant graft-modified ethylene/propylene block copolymer may be used as it is or after it has been mixed with the above-mentioned unmodified ethylene/propylene block copolymer so that the polar monomer content in the mixture is at least 0.05% by weight, preferably 0.05 to 1% by weight. It is preferred that the MFR of the thus-obtained modified ethylene/propylene block copolymer be 1 to 150 g/10 min.
In the present invention, a polyolefin rubber may be incorporated. As the polyolefin rubber, there can be preferably used an ethylene/propylene copolymer rubber (EPR) having an ethylene content of about 30 to about 80% by weight, an ethylene/propylene/nonconjugated diene copolymer rubber (EPDM), and an ethylene/butene- 1 copolymer rubber. Of these, the ethylene/propylene copolymer rubber is most preferable. The polyolefin rubber may be graft-modified with a polar monomer as mentioned above. The method for introducing the polar monomer by graft modification is not particularly critical. For example, the introduction can be accomplished according to a solution method or heat-kneading method using a radical initiator such as an organic peroxide as mentioned above. It is preferred that the polar monomer be grafted to the polyolefin rubber for the modification in an amount of 0.05 to 3.5% by weight. After the graft modification, the graft-modified polyolefin rubber can be recovered according to known procedures. It is preferred that the ML1+4 value (100°C) of the graft-modified polyolefin rubber be in the range of from 10 to 100.
In the present invention, a surface-treated glass fiber is used. The shape or length of the glass fiber is not particularly critical. A chopped strand having a diameter of 3 to 30μ and a length of 2 to 10 mm, or a roving, may be used. As the surface-treating agent used for the surface treatment, there can be mentioned vinyltriethoxysilane, vinyltris(β-methoxyethoxy)silane, γ-methacryloxypropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, n-(dimethoxymethylsilylpropyl)ethylenediamine, n-(triemthoxysilylpropyl)ethylenediamine, γ-aminopropyltriethoxysilane and γ-aminopropyltrimethoxysilane. It is preferred that the amount of the surface-treating agent be 0.05 to 3% by weight. A commercially available surface-treated glass fiber may be used as it is.
The mixing ratios of the respective components in the glass fiber-reinforced polypropylene composition are such that the amount of the modified ethylene/propylene block copolymer (A) is 99 to 40% by weight, preferably 85 to 50% by weight, the amount of the polyolefin rubber (B) is up to 20% by weight, preferably 3 to 20% by weight, and the amount of the surface-treated glass fiber (C) is 1 to 45% by weight, preferably 5 to 45% by weight, more preferably 10 to 30% by weight. If the amount of the glass fiber is smaller than the lower limit, the reinforcing effect is low and the heat distortion temperature and rigidity of the molded article are reduced. If the amount of the glass fiber is larger than the upper limit, the flowability of the composition is reduced and the appearance of the molded article is degraded. If the amount of the polyolefin rubber exceeds the upper limit, the heat distortion temperature and rigidity of the molded article are reduced.
Known additives may be added to the glass fiber-reinforced polypropylene composition of the present invention. For example, there may be added pigments, antioxidants, ultraviolet absorbers, flame retardants, antistatic agents, lubricants, nucleating agents, organic and inorganic fillers such as talc, calcium carbonate, mica, barium sulfate, (calcined) kaolin, silica, magnesium silicate, zeolite, carbon fiber, aromatic polyamide fiber, potassium titanate fiber, asbestos fiber, metal fiber, and boron fiber, and other thermoplastic resins such as nylon, polyester and polycarbonate, in so far as there is no adverse influence on the physical properties of the glass fiber-reinforced polypropylene composition. The amounts of these additives are appropriately determined based on the results of experiments.
In the case where the glass fiber is a chopped strand, the glass fiber-reinforced polypropylene composition of the present invention can be prepared by kneading the above-mentioned components by an extruder, a Banbury mixer, an intensive mixer or the like. When the polyolefin rubber is used, the composition is preferably obtained by melt-kneading the graft-modified crystalline ethylene/propylene block copolymer (optionally together with the unmodified crystalline ethylene/propylene block copolymer) and the polyolefin rubber by a twin-screw extruder and kneading the obtained molten polymer mixture with the glass fiber by a single screw extruder. According to this method, breaking of the glass fiber is controlled and good results are obtained.
The glass fiber-reinforced polypropylene composition of the present invention can be used in fields where a high rigidity and impact resistance are required, for example, for automobile parts, electric appliances, construction materials, and industrial parts.
The present invention will now be described in detail with reference to the following examples and comparative examples. In these examples, all of "parts" and "%" are by weight.
In the examples, the ethylene content in the polymer was determined by the infrared spectrophotometry. With respect to injection-molded test pieces, the tensile strength was determined according to ASTM D-638, the flexural modulus was determined according to ASTM D-790, the heat distortion temperature was determined according to ASTM D-648 (at 18.6 kg/cm2), and the Izod impact strength (notched) was determined according to D-256 (at 23°C). The appearance of the molded article was evaluated based on the gloss and surface roughness and on whether or not the glass fiber rose on the surface; the mark "A" indicates a good appearance, mark "B" indicates a slightly bad appearance, and mark "C" indicates a bad appearance.
In a tumbler, 100 parts of a crystalline ethylene/propylene block copolymer or crystalline propylene homopolymer shown in Table 1 was homogeneously mixed with 0.5 part of itaconic anhydride and 0.15 part of t-butyl peroxybenzoate, and the graft modification was carried out at a temperature of 200°C in a single screw extruder having a diameter of 65 mm for a residence time of 2 minutes, followed by pelletization, to obtain graft-modified polypropylene (the grafting ratio was 0.36% in Example 1).
In a tumbler, 80 parts of this graft-modified polypropylene was mixed with 20 parts of a glass fiber having a diameter of 10 μm and a length of 6 mm, treated with 0.1% of aminosilane, and by using a single screw extruder having a diameter of 65 mm, and the mixture was kneaded at a temperature of 220°C for a residence time of 2 minutes, followed by pelletization, to obtain a pellet of a glass fiber-reinforced polypropylene composition having a diameter of 3 mm and a length of 5 mm.
A test piece obtained by injection-molding this pellet was evaluated. The obtained results are shown in Table 1.
| TABLE 1 |
| __________________________________________________________________________ |
| Comparative |
| Comparative |
| Comparative |
| Comparative |
| Example 1 |
| Example 1 |
| Example 2 |
| Example |
| Example |
| __________________________________________________________________________ |
| 4 |
| Crystalline |
| MFR (g/10 min) 2 2 2 2 2 |
| polypro- |
| Ethylene content (%) |
| 6.0 9.6 15.6 2.5 0 |
| pylene Intrinsic viscosity of portion soluble |
| 4.0*1 |
| 10.7 3.2 2.7 -- |
| in p-xylene at normal temperature |
| Ethylene content in portion insoluble in |
| 4.3 7.6 14.6 1.3 -- |
| p-xylene at normal temperature (%) |
| Physical |
| Tensile strength (kg/cm2) |
| 640 600 580 650 880 |
| properties |
| Flexural modulus (kg/cm2) |
| 33,000 30,000 28,000 33,000 38,000 |
| Heat distortion temperature (°C.) |
| 141 136 135 143 153 |
| Izod impact strength (kg · cm/cm) |
| 15 12 9 8 9 |
| H.S.I.*2 (kg · cm) |
| 110 60 40 10 0 |
| Appearance of molded article |
| A B C A A |
| General evaluation A C C C C |
| __________________________________________________________________________ |
| Note |
| 1 The proportion of the portion soluble in pxylene at |
| normaltemperature was 9%. |
| 2 The H.S.I. value was determined according to the Ube method |
| (falling missile impact strength, which is a kind of drop weight impact |
| strength). The value indicates the energy required for breaking the test |
| piece when a missile having a top end diameter of 1 inch was caused to |
| impact at a speed of 2.5 m/sec on the test piece, which was an |
| injectionmolded disk having a thickness of 3 mm and a diameter of 100 mm. |
Note
(1) The proportion of the portion soluble in p-xylene at normal temperature was 9%.
(2) The H.S.I value was determined according to the Ube method (falling missile impact strength, which is a kind of drop weight impact strength). The value indicates the energy required for breaking the test piece when a missile having a top end diameter of 1 inch was caused to impact at a speed of 2.5 m/sec on the test piece, which was an injection-molded disk having a thickness of 3 mm and a diameter of 100 mm.
A glass fiber-reinforced polypropylene composition (pelletized) was obtained from 70 parts of the graft-modified polypropylene obtained in Example 1, 10 parts of graft-modified EPR (ethylene content=75%, Mooney viscosity ML1+4 (100°C)=80, maleic anhydride grafting ratio=1%) obtained by carrying out graft modification at 135°C for 4 hours with dicumyl peroxide as the catalyst in o-dichlorobenzene, 20 parts of the same glass fiber as used in Example 1, 0.2 PHR (based on polypropylene) of Irganox 1010 (trademark, hindered phenol antioxidant) and 0.1 PHR (based on polypropylene) of BHT by using a continuous two-stage extruder. In the first stage of the extruder, mixing of the polymer components was carried out by using a twin screw extruder at 200° to 240°C, and, in the second stage of the extuder, mixing of the polymer mixture with glass fiber was carried out by using a 65 mm-diameter single screw extruder while a glass fiber is supplied from feed portion of the single screw extruder, at a mixing temperature of 200° to 280°C
The composition was evaluated in the same manner as described in Example 1. It was found that the tensile strength was 590 kg/cm2, the flexural modulus was 30,000 kg/cm2, the heat distortion temperature was 136°C, the Izod impact strength was 25 kg.cm, the H.S.I value was 200 kg.cm, the appearance of the molded article was good, and the general evaluation was good (A).
A box-shaped molded article having a length of 500 mm, a width of 150 mm, and a height of 200 mm was prepared from the glass fiber-reinforced polypropylene (pellet) obtained in Example 1 (Example 3), Example 2 (Example 4), or Comparative Example 1 (Comparative Example 5) by using an injection molding machine (Model UBE MAX 415-50 supplied by Ube Industries).
With respect to each injection-molded article, 10 test pieces were tested in the following manner. Namely, a steel ball having a weight of 1 kg was allowed to fall from a height of 1 m onto the surface of the sample at -10°C The number of the samples where cracking or breaking occurred was checked. In Example 3, no sample was cracked or broken, and in Example 4 no sample was cracked or broken, but 10 samples were cracked or broken in Comparative Example 5.
As is apparent from the foregoing description, a glass fiber-reinforced polypropylene composition having an excellent rigidity and impact strength can be obtained by a simple operation according to the present invention.
Kita, Yasuo, Morita, Hideyo, Akagawa, Tomohiko
| Patent | Priority | Assignee | Title |
| 10131785, | Jun 30 2015 | Lotte Chemical Corporation | Polyester resin composition with excellent impact resistance and light reliability and molded article using the same |
| 10301449, | Nov 29 2013 | Lotte Chemical Corporation | Thermoplastic resin composition having excellent light stability at high temperature |
| 10508190, | Dec 17 2014 | Lotte Chemical Corporation | Polyester resin composition and molded article manufactured therefrom |
| 10538661, | Jun 30 2015 | Lotte Chemical Corporation | Polyester resin composition with excellent impact resistance and light reliability and molded article using the same |
| 10636951, | Jun 27 2014 | Lotte Chemical Corporation | Thermoplastic resin composition having excellent reflectivity |
| 10822490, | Dec 30 2013 | Lotte Chemical Corporation | Thermoplastic resin composition having excellent shock resistance and light resistance |
| 11355683, | Jun 27 2014 | Lotte Chemical Corporation | Thermoplastic resin composition having excellent reflectivity |
| 4983647, | Nov 08 1988 | Ube Industries, Ltd. | Reinforced polypropylene composition |
| 5039718, | May 22 1987 | Imperial Chemical Industries PLC | Fillers |
| 5376701, | Jan 15 1990 | AZDEL, INC | Thermoplastic polymer fibre composition |
| 5484835, | May 31 1993 | S O I TEC SILICON ON INSULATOR TECHNOLOGIES, S A | Heat-resistant, propylene resin-based molding materials and molded products obtained therefrom |
| 5707734, | Jun 02 1995 | Owens-Corning Fiberglas Technology Inc | Glass fibers having fumed silica coating |
| 6521693, | Mar 01 2000 | JNC Petrochemical Corporation | Long fiber-reinforced polypropylene resin composition and molded article |
| 6867252, | Mar 10 1999 | PRIME POLYMER CO , LTD | Propylene resin composition and interior automotive member comprising the same |
| 7226955, | Feb 22 2002 | SEALED AIR CORPORATION US | Macrocellular acoustic foam containing particulate additive |
| 8664322, | Sep 29 2006 | LOTTE ADVANCED MATERIALS CO , LTD | Thermoplastic resin composition and plastic article |
| 9150704, | Jun 21 2011 | LOTTE ADVANCED MATERIALS CO , LTD | Polyester resin composition |
| 9359500, | Dec 28 2012 | LOTTE ADVANCED MATERIALS CO , LTD | Resin compositions and articles including the same |
| 9437790, | Dec 28 2011 | LOTTE ADVANCED MATERIALS CO , LTD | Polyester resin composition having good yellowing resistance and impact resistance |
| 9493648, | Dec 28 2012 | LOTTE ADVANCED MATERIALS CO , LTD | Thermoplastic resin compositions and molded products including the same |
| RE44893, | Mar 26 2004 | Hanwha Azdel, Inc. | Fiber reinforced thermoplastic sheets with surface coverings |
| Patent | Priority | Assignee | Title |
| 4439573, | Dec 25 1981 | Ube Industries, Ltd | Propylene polymer composition |
| 4480065, | Jun 04 1982 | Mitsui Chemicals, Inc | Polypropylene-base resin composition |
| 4621115, | Apr 27 1984 | NISSAN MOTOR CO , LTD | Glass fiber reinforced polypropylene compositions comprising crystalline e-p block copolymer graft modified with itaconic anhydride |
| GB2097408, | |||
| JP37036, | |||
| JP104136, | |||
| JP592294, |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Feb 10 1986 | MORITA, HIDEYO | Ube Industries, Ltd | ASSIGNMENT OF ASSIGNORS INTEREST | 004519 | /0947 | |
| Feb 10 1986 | AKAGAWA, TOMOHIKO | Ube Industries, Ltd | ASSIGNMENT OF ASSIGNORS INTEREST | 004519 | /0947 | |
| Feb 10 1986 | KITA, YASUO | Ube Industries, Ltd | ASSIGNMENT OF ASSIGNORS INTEREST | 004519 | /0947 | |
| Feb 18 1986 | Ube Industries, Ltd. | (assignment on the face of the patent) | / | |||
| Feb 16 1993 | Ube Industries, Ltd | NISSAN MOTOR CO , LTD | ASSIGNMENT OF ONE-HALF INTEREST | 006451 | /0715 |
| Date | Maintenance Fee Events |
| Nov 02 1990 | M173: Payment of Maintenance Fee, 4th Year, PL 97-247. |
| Mar 06 1995 | M184: Payment of Maintenance Fee, 8th Year, Large Entity. |
| Feb 03 1999 | M185: Payment of Maintenance Fee, 12th Year, Large Entity. |
| Date | Maintenance Schedule |
| Sep 15 1990 | 4 years fee payment window open |
| Mar 15 1991 | 6 months grace period start (w surcharge) |
| Sep 15 1991 | patent expiry (for year 4) |
| Sep 15 1993 | 2 years to revive unintentionally abandoned end. (for year 4) |
| Sep 15 1994 | 8 years fee payment window open |
| Mar 15 1995 | 6 months grace period start (w surcharge) |
| Sep 15 1995 | patent expiry (for year 8) |
| Sep 15 1997 | 2 years to revive unintentionally abandoned end. (for year 8) |
| Sep 15 1998 | 12 years fee payment window open |
| Mar 15 1999 | 6 months grace period start (w surcharge) |
| Sep 15 1999 | patent expiry (for year 12) |
| Sep 15 2001 | 2 years to revive unintentionally abandoned end. (for year 12) |